General Responsibilities
Project Initiation, Planning, Execution and Monitoring, Closing
* Define project scope, objectives, deliverables, and success criteria in collaboration with stakeholders
* Planning, execution, monitoring of software and hardware new product development projects for medical devices using a hybrid approach, integrating agile methodologies for software innovation and waterfall frameworks for hardware development
* Develop comprehensive project plans, encompassing timelines, budgets, and resource allocation
* Monitor project progress, identify and manage risks, and implement contingency plans to ensure objectives are met
* Plan and monitor assigned budget
* Ensure adherence to design controls and product development processes
Cross-functional collaboration
* Ensure effective identification and communication of goals, progress, risks and issues
Regulatory and Compliance Oversight
* Ensure all project activities adhere to medical device regulatory requirements (e.g. ISO 13485)
* Maintain documentation in compliance with quality management systems
Skills and Experience
* Bachelor’s degree in engineering, Business, or related field
* Project Management Expertise: some years managing end-to-end product development projects in the medical device industry is a "must"
* SW Project Management Knowledge: Familiarity in project management of Medical Device Software (according to IEC 62304)
* Regulated Industry Knowledge: Familiarity with product development processes, including design controls, in compliance-driven environments
* Collaboration & Communication: Strong interpersonal and motivational skills to foster teamwork and alignment across functions and levels
* Problem-solving: Resilience, adaptability, and a proactive approach to navigating challenges
* Technical Proficiency: Experience with project management methodologies (e.g., Agile, Waterfall) and tools like MS Project or similar platforms
* Prior experience in product development or engineering within the medical device industry
* Basic understanding of medical device standards and regulations
* PMP certification is desirable
* Scrum Master experience is desirable
* Fluent English language skills, written and spoken
What we can offer you
In addition to providing you with a supportive, inclusive and collaborative environment where you will feel empowered to take ownership and drive meaningful change, we will reward you with the following:
* A dynamic role in an advanced Medical Device environment interfacing with all worldwide regulatory landscapes supporting your professional career growth
* Exposure to a State-of-the-Art medical device development process, in close co-operation with international clinicians
* Competitive base salary
* Variable short-term & long-term incentives
* Recognition: through our STARS Program, we recognize and celebrate our colleagues’ contributions and achievements
If you like the sound of the above and feel energized by the idea of joining a great brand at a moment of exciting expansion, please apply now. We look forward to hearing from you!